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Journal Abstract Search

188 related items for PubMed ID: 8010712

  • 1. Cytogenetic characterization of cat eye syndrome marker chromosome.
    Wenger SL, Surti U, Nwokoro NA, Steele MW.
    Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
    [Abstract] [Full Text] [Related]

  • 2. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M, Visedo G, Sanchís A, Sentís C, Villa A, Ludeña P, Hortigüela JL, Martínez-Frías ML, Fernández-Piqueras J.
    Am J Med Genet; 1994 Jan 01; 49(1):77-82. PubMed ID: 8172255
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  • 3. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O, Rasi S, Hoffmann K, Blin N.
    Eur J Hum Genet; 2005 May 01; 13(5):592-8. PubMed ID: 15756300
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  • 4. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF, Wyandt H, Huang XL, Milunsky JM.
    Clin Genet; 2005 Aug 01; 68(2):146-51. PubMed ID: 15996211
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  • 5. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM.
    Exp Mol Pathol; 2006 Jun 01; 80(3):262-6. PubMed ID: 16516886
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL, Brothman AR, Carey JC, Chance PF.
    Am J Med Genet; 1996 May 03; 63(1):250-6. PubMed ID: 8723118
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  • 7. Mosaic 5p tetrasomy.
    Stanley WS, Powell CM, Devine GC, Ellingham T, Samango-Sprouse CA, Vaught DR, Murphy BA, Rosenbaum KN.
    Am J Med Genet; 1993 Mar 15; 45(6):774-6. PubMed ID: 8456861
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  • 8. Cat-eye syndrome with different marker chromosomes in a mother and daughter.
    Ing PS, Lubinsky MS, Smith SD, Golden E, Sanger WG, Duncan AM.
    Am J Med Genet; 1987 Mar 15; 26(3):621-8. PubMed ID: 3105314
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  • 12. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
    Knoll JH, Asamoah A, Pletcher BA, Wagstaff J.
    Am J Med Genet; 1995 Jan 16; 55(2):221-4. PubMed ID: 7717422
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  • 13. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH.
    Delneste D, Vamos E, Pierquin G, Hayez-Delatte F, Van Regemorter N.
    Genet Couns; 1998 Jan 16; 9(2):97-102. PubMed ID: 9664205
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  • 16. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
    Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T.
    Med Wieku Rozwoj; 2006 Jan 16; 10(1 Pt 2):211-25. PubMed ID: 17028390
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  • 17. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Jan 16; 48(1):27-33. PubMed ID: 8815483
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